Chronocoulometric Quantum Dot Aptasensor for SARS‐CoV‐2 Nucleocapsid Protein Biomarker

Author:

Sanga Nelia A.1ORCID,Oranzie Marlon1ORCID,Leve Zandile1ORCID,Januarie Kaylin C.1ORCID,Mokwebo Kefilwe V.1ORCID,Uhuo Onyinyechi V.1ORCID,Ross Natasha1ORCID,Douman Samantha F.12ORCID,Pokpas Keagan1ORCID,Iwuoha Emmanuel I.1ORCID

Affiliation:

1. SensorLab (University of the Western Cape Sensor Laboratories) University of the Western Cape Robert Sobukwe Road, Bellville 7535 Cape Town South Africa

2. Department of Chemistry University of Cape Town, Rondebosch Cape Town 7700 South Africa

Abstract

AbstractFor the first time, a novel mercaptosuccinic acid‐capped tungsten telluride quantum dot (MSA‐WTe3‐QD)‐based electrochemical aptasensor was designed for the determination of SARS‐CoV‐2 N‐protein in synthetic human serum, plasma and urine. The MSA‐WTe3‐QD which exhibited spherical morphology and an average diameter of 3.56 nm were synthesized through a bottom‐up approach. The aptasensor was prepared by firstly immobilizing MSA‐WTe3‐QD on a screen‐printed carbon electrode (SPCE) by using the 1‐ethyl‐3‐(3‐dimethylaminopropyl)carbodiimide/N‐hydroxysuccinimide (EDC/NHS) coupling chemistry. Thereafter, amine‐terminated 90‐mer ssDNA aptamer was deposited on the modified SPCE and left to cure to form the aptasensor. Using the chronocoulometry signal transduction technique, the aptasensor's calibration with N‐protein gave a linear range value of 1–9 pg.mL−1 and a limit of detection (LOD) value of 0.08 pg.mL−1. The LOD value of the aptasensor was 8 times lower than the LOD value of 0.71 pg.mL−1 obtained with a commercial N‐protein ELISA kit. When tested in simulated real samples the aptasensor recovery rates of 95–103.33 % were obtained. In the presence of various interferents, the aptasensor displayed good selectivity to N‐protein.

Publisher

Wiley

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